EP1209132A1 - Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren - Google Patents

Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren Download PDF

Info

Publication number
EP1209132A1
EP1209132A1 EP00204144A EP00204144A EP1209132A1 EP 1209132 A1 EP1209132 A1 EP 1209132A1 EP 00204144 A EP00204144 A EP 00204144A EP 00204144 A EP00204144 A EP 00204144A EP 1209132 A1 EP1209132 A1 EP 1209132A1
Authority
EP
European Patent Office
Prior art keywords
coating
less
mpa
primary coating
cavitation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00204144A
Other languages
English (en)
French (fr)
Inventor
Markus Johannes Henricus Bulters
Gerrit Rekers
Philippe Wolfgang Paul Valere Bleiman
Jozef Maria Herman Linsen
Alexander Antonius Marie Stroeks
Johannes Adrianus Van Eekelen
Adrianus Gijsbertus Maria Abel
Marko Dorschu
Paulus Antonius Maria Steeman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Koninklijke DSM NV
Original Assignee
DSM NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by DSM NV filed Critical DSM NV
Priority to EP00204144A priority Critical patent/EP1209132A1/de
Priority to CNA018221807A priority patent/CN1486349A/zh
Priority to BR0115549-0A priority patent/BR0115549A/pt
Priority to CNB018070361A priority patent/CN1257003C/zh
Priority to AT01997528T priority patent/ATE302823T1/de
Priority to JP2002545092A priority patent/JP2004514759A/ja
Priority to DE60112965T priority patent/DE60112965D1/de
Priority to US09/989,717 priority patent/US6916855B2/en
Priority to JP2002544378A priority patent/JP4268406B2/ja
Priority to KR1020027009364A priority patent/KR100854847B1/ko
Priority to AU2002222795A priority patent/AU2002222795A1/en
Priority to CNB2006100726945A priority patent/CN100545685C/zh
Priority to PCT/NL2001/000850 priority patent/WO2002042237A2/en
Priority to US09/989,703 priority patent/US7067564B2/en
Priority to EP01997528A priority patent/EP1341857B1/de
Priority to KR10-2003-7006878A priority patent/KR20030055316A/ko
Priority to EP01997468.2A priority patent/EP1274662B1/de
Priority to PCT/NL2001/000849 priority patent/WO2002042383A1/en
Priority to AU2002222796A priority patent/AU2002222796A1/en
Publication of EP1209132A1 publication Critical patent/EP1209132A1/de
Priority to US11/109,949 priority patent/US20050187310A1/en
Priority to US11/269,765 priority patent/US7706659B2/en
Priority to JP2008139946A priority patent/JP4594999B2/ja
Priority to US12/591,242 priority patent/US7865055B2/en
Priority to US12/591,241 priority patent/US7886612B2/en
Withdrawn legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/48—Coating with two or more coatings having different compositions
    • C03C25/50—Coatings containing organic materials only
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/104—Coating to obtain optical fibres
    • C03C25/106—Single coatings
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
    • C08F230/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing phosphorus
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805—Compounds having only one group containing active hydrogen
    • C08G18/2815—Monohydroxy compounds
    • C08G18/284—Compounds containing ester groups, e.g. oxyalkylated monocarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/2805—Compounds having only one group containing active hydrogen
    • C08G18/285—Nitrogen containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C08G18/671—Unsaturated compounds having only one group containing active hydrogen
    • C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/8064—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with monohydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/81—Unsaturated isocyanates or isothiocyanates
    • C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
    • C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
    • C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
    • C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/02—Optical fibres with cladding with or without a coating
    • G02B6/02395—Glass optical fibre with a protective coating, e.g. two layer polymer coating deposited directly on a silica cladding surface during fibre manufacture
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
    • C08F222/10—Esters
    • C08F222/1006—Esters of polyhydric alcohols or polyhydric phenols
    • C08F222/106—Esters of polycondensation macromers
    • C08F222/1065—Esters of polycondensation macromers of alcohol terminated (poly)urethanes, e.g. urethane(meth)acrylates
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/44—Mechanical structures for providing tensile strength and external protection for fibres, e.g. optical transmission cables
    • G02B6/4401—Optical cables
    • G02B6/4403—Optical cables with ribbon structure

Definitions

  • the present invention relates to a coated optical fiber comprising a primary and secondary coating, to a radiation curable primary coating composition, to a combination of a primary and secondary coating, and to a ribbon comprising at least one of said coated optical fibers and to a method and apparatus for measuring cavitation strength of a coating for use as a primary coating on an optical fiber.
  • optical fibers are fragile and easily broken, the optical fibers are usually coated with a coating material which is a radiation curable resin composition.
  • the transmission characteristics of optical fibers are known to be significantly affected by properties such as modulus or the like of the primary coating material which is in direct contact with the optical fibers.
  • a primary coating material having an equilibrium modulus of about 2 MPa or higher the transmission loss of the optical fibers may increase because of decreased buffering effect.
  • a material having a low modulus of elasticity is, therefore, desirable as the primary coating material.
  • Primary coating materials having an equilibrium modulus of 1.5 MPa or less are thus of interest as is described for example by Bouten et al. (J. of Lightwave Technology, Vol. 7 April 1989, p.680-686).
  • these coatings need further improvement in strength or integrity because defects still appear during the use of the coated optical fiber, in particular, under the influence of high stresses and temperature extremes which the coated fiber has to withstand over time (during production, cabling or when buried under the ground). This problem is further enhanced nowadays due to the increasing line speeds for fiber drawing causing steeper cooling profiles, and allowing less time for relaxation.
  • a primary coating having an equilibrium modulus of about 1.5 MPa or lower when coated on a glass optical fiber and when subsequently having a secondary coating (having a much higher Tg) applied thereon, undergoes at least the following stress: when the temperature decreases during the production process the secondary coating passes its glass temperature (Tg) and enters the glassy state while the primary coating is still above it's glass temperature.
  • Tg glass temperature
  • the primary coating still intends to shrink when the temperature decreases further, but is captured between the rigid secondary on the one hand and the rigid glass substrate on the other hand. This precludes the shrinking process of the primary coating substantially.
  • the present inventors realized that the integrity of a soft primary coating in a coated optical fiber during use is (a.o.) dependent on its resistance to cavitation.
  • the present invention relates to a coated optical fiber having a primary coating which sufficiently adheres to the optical fiber to reduce to a minimum the occurrence of delaminations (or debonding) at the primary coating-glass interface and wherein the secondary coating sufficiently adheres to the primary coating to reduce to a minimum the occurrence of delaminations at the primary coating-secondary coating interface, wherein said primary coating has a cavitation strength that is sufficient to reduce to a minimum the occurrence of delaminations or cavitations within the coating itself.
  • the present invention provides a coated optical fiber having a primary coating having a cavitation strength of at least 1.40 of its dynamic modulus at 23°C (E' 23 ), but at least 1.0 MPa, while having sufficient adhesion to glass.
  • a suitable definition of the phenomenon of cavitation strength according to the present invention is the stress at which the tenth cavitation becomes visible when measured in a tensile testing machine at a pulling speed of 20 ⁇ m/min for a 100 ⁇ m thin layer (or 20% per min) when observed at a magnification of about 20x.
  • the present invention furthermore provides a coated optical fiber comprising said primary coating and a secondary coating having a Tg of about 40°C or more and a modulus (1 Hz; dynamic modulus E' at 23°C) of about 400 MPa or more.
  • the present invention furthermore provides a primary coating having above defined cavitation strength, furthermore the invention provides a primary coating having sufficient strain hardening to substantially increase the resistance to cavitation of the primary coating in comparison to a coating exhibiting "ideal Gaussian rubber” characteristics and/or a sufficient strain energy release rate (Go).
  • the present invention provides a primary coating having a sufficient low expansion coefficient while having a low modulus and an improved combination of expansion coefficient for a primary-secondary coating system.
  • the present invention further provides an apparatus for measuring the cavitation strength of a coating and a method for measuring said cavitation strength of a coating for use as a primary coating on an optical glass fiber.
  • Photograph 1 shows the set up for a cavitation strength measurement.
  • Photograph 2 shows the top fixture of the cavitation strength measurement set up.
  • Photograph 3 shows sample of two primary coatings with cavities.
  • Photograph 4 shows the micrometer set-up used for the sample preparation for the cavitation strength measurement.
  • Figure 1 schematically shows an apparatus used for determining the cavitation strength of a sample.
  • Figure 2 shows the sample geometry in the cavitation set-up.
  • Figure 3 shows the cavitation strength at the tenth cavitation as a function of E'23.
  • Figure 4 shows the number of cavitations at increasing stresses on a primary coating sample with precure (0.96 J/cm 2 + 3 precure flashes) and a sample without precure (0.93 J/cm 2 ) (speed 20%/min).
  • Figure 5 shows relative Mooney plots of several primary coatings.
  • the primary coating of the present invention has an equilibrium modulus of about 1.5 MPa or less.
  • the equilibrium modulus according to the present invention is measured by DMTA in tension according to ASTM D5026-95a, wherein the modulus is determined as described in the experimental section.
  • Use of such a low modulus primary coating results in an increased resistance against attenuation of the light transported through the glass fiber. This resistance against attenuation is in particular relevant in so called “non zero dispersion shifted single mode optical fibers", and in multimode fibers as these fibers are sensitive to attenuation due to so-called microbending.
  • the equilibrium modulus is about 1.3 MPa or less, more preferred about 1.0 MPa or less, even more preferred about 0.9 MPa or less, and most preferred, about 0.8 MPa or less.
  • the modulus will be about 0.05 MPa or higher, preferably about 0.1 MPa or higher, more preferably about 0.2 MPa or higher, and most preferred, about 0.3 MPa or higher.
  • the resistance to cavitation (further called cavitation strength) should be sufficiently high.
  • the present invention now provides primary coatings fulfilling the above requirements.
  • the present invention also provides a method and an apparatus for measuring the cavitation strength, which is the stress at which a defined number of cavitations becomes visible at about 20x magnification.
  • the stress is measured at which a second, fourth, or tenth cavitation becomes visible at about 20x magnification at a pulling speed of 20 ⁇ m/min in a 100 ⁇ m thick sample (or 20% min -1 ).
  • This method and apparatus can then be used to design the primary coatings of the present invention.
  • the apparatus for measuring the cavitation strength of a coating according to the present invention comprises an assembly comprising:
  • Figure 1 schematically shows an apparatus that may be used for determining the cavitation strength of a sample (30), in particular an ultraviolet cured film of ultraviolet curable material.
  • the set up includes a tensile testing apparatus comprising an assembly for holding a sample for testing.
  • the tensile testing apparatus comprises a load cell (50) for measuring the force that is required to move a moving plate (80) in a normal direction apart from a stationary plate (70). Load cell (50) is attached to the stationary plate (70). The movement of the plate (80) may be guided by bars or a set of bars (100).
  • the tensile testing apparatus may further comprise a displacement transducer (90), which can regulate the speed with which the plate (80) is displaced from the stationary plate (70).
  • the assembly comprises a first member (10) having a first surface and a second member (20) with a second surface facing said first surface.
  • said load cell (50) can register the force that is required to move said first surface in a direction normal towards said second surface and said displacement transducer can regulate the speed at which said first surface is normally moved from said second surface.
  • the first and second surface define an area for holding a sample (30).
  • at least one of the first member and second member is made of a material that is transparent to ultraviolet (UV) light. Materials that are transparent to UV light are well-known in the art and include, for instance, quartz glass.
  • at least the second member (20) is made of UV transparent material.
  • the assembly is capable of receiving a UV curable composition which may be cured in situ.
  • both the first and the second member are transparent to the naked eye.
  • the second member is adapted to be attached to load cell (50).
  • the assembly further comprises a sub-assembly for positioning the first member (10) in a position perpendicular to the direction of the force applied to the sample (30).
  • the sub-assembly has at least one element (40) that can adjust the position of the first member (10) relative to the direction in which the moving plate (80) is displaceable.
  • Such an element may be, for instance, an adjustment screw.
  • the sub-assembly comprises at least two adjustment screws, more preferably at least three adjustment screws, and most preferred, at least three micrometer screws on the moving plate and three hardened steel balls fitted to the adjustable plate.
  • the sub-assembly further comprises a ring plate (110) attached to the moving plate (80).
  • the plate is preferably constructed such that it is sufficiently rigid to minimize or eliminate any effect on the measuring of the sample during testing.
  • the plate (80) may be constructed from rigid steel.
  • a bore extends through the plate (110), and also through the moving plate (80), to allow the sample (30) to contact both said first surface of the first member (10) and said second surface of the second member (20).
  • First member (10) is attached to or rests on the ring plate (110).
  • An example of how the sub-assembly can adjust the position of the first member (10) relative to the movement of the plate (80) is given below:
  • the adjustment elements (40) in Figure 1 could be, for example, adjustment screws, such as micrometer screws. Adjusting one of the screws will cause the ring plate (110) to change its angle (or tilt) with respect to the direction of movement (or force imposed on the sample during testing). Since the first member (10) is attached to or rests on the ring plate (110), the first member (10) will also change its angle (or tilt) relative to moving plate (80). Accordingly, the position of the first member (10) relative to the moving direction of the moving plate (80) is adjusted.
  • One of the benefits of the sub-assembly is that it be used to ensure that the position of said first surface of the first member (10) is perpendicular to the moving direction of the moving plate (80).
  • said sub-assembly is capable of adjusting the position in such a manner that both the first member and the second member are perpendicular to the direction of the normal movement or moving direction of the moving plate (80) or, in other words, are parallel to each other (further called parallelity adjustment).
  • the set up in Figure 1 further comprises a viewer (60) for optically observing and/or recording a contacting surface of the sample (30) in a direction parallel to the moving direction of the moving plate (80).
  • a viewer for optically observing and/or recording a contacting surface of the sample (30) in a direction parallel to the moving direction of the moving plate (80).
  • Such viewer (or viewing means) (60) may be any device suitable for observing the surface contacting either the first or second surface and/or the sample in between.
  • the viewer includes a magnifier, such as, for instance, a microscope, a video camera, and/or a microscope in conjunction with a video camera.
  • the present invention further relates to a tensile testing apparatus comprising the assembly as described above.
  • Said tensile testing apparatus comprising said assembly has a compliance of less than about 0.5 ⁇ m/N, preferably, of about 0.4 ⁇ m/N or less, more preferred, about 0.3 ⁇ m/N or less, and most preferred about 0.2 ⁇ m/N or less.
  • the apparatus is used for measuring the cavitation strength of a primary optical glass fiber coating and comprises, a tensile testing machine having a fixed plate to which a load cell with a lower end sample part (second member (20)) can be fixed, optionally further comprising a displacement transducer, and comprising a moving plate and a top fixture; either the top (first member (10)) sample part or lower sample part (second member (20)) being provided with means to adjust the parallelity of the sample to be perpendicular to the direction of the normal movement (see Photograph 2), the apparatus being further provided with a microscope and preferably also a recorder fitted on said top (moving) plate, the compliance of the total set up of the apparatus being less than about 0.5 ⁇ m/N (preferred ranges see above) and wherein the thickness of said top and lower sample part are about 2 mm or more, preferably, about 3 mm or more, more preferably, about 4 mm or more.
  • the method for measuring the cavitation strength according to the present invention comprises the steps of:
  • the coating is cured with such UV-dose that the coating attains at least 85% of its equilibrium modulus (preferably, at least 90%, more preferred, at least 95%). It is preferred to cure the coating with a UV-dose of about 1 J/cm 2 .
  • the method for measuring the cavitation strength comprises the steps of:
  • Photograph 3 shows the appearance of cavities in two samples of primary coatings A and B in a cavitation measurement as a function of the force applied.
  • the cavities can have different forms depending on the type of primary coating.
  • Coating A shows bubble-like cavities whereas coating B shows stripe-like cavities.
  • the measurement preferably is performed by videorecording the sample during the measurement.
  • the measurement can be performed with a 100 ⁇ m thin layer, for which the pulling speed of 20 ⁇ m/min can be used to obtain a deformation rate of 0.20 min -1 .
  • the deformation rate can be defined by the pulling speed divided by the layer thickness.
  • the stress at which, the second, fourth or tenth cavitation becomes visible is taken as the cavitation strength of a coating.
  • the tenth cavitation is used as the measuring point.
  • the cavitation strength at which the tenth cavity appears preferably is 1.0 MPa or higher as measured at a deformation rate of 0.20 min -1 , of a primary coating sample which has been prepared according to the method described in detail in the experimental section and the cavitation strength preferably is at least is 1.4 times the dynamic modulus at 23°C (E' 23 ) of said primary coating (see Figure 3).
  • the present invention relates to a primary coating composition when cured having an equilibrium modulus of about 1.5 MPa or less and a cavitation strength at which a tenth cavitation appears ( ⁇ 10 cav ) of at least about 1.0 MPa as measured at a deformation rate of 0.20% min -1 , said cavitation strength being at least about 1.4 times said dynamic modulus at 23°C (E' 23 ).
  • the cavitation strength is at least about 1.5 times the modulus, more preferably at least about 1.6 times the modulus.
  • the stress which is exerted (in actual use) on the primary coating further depends on the secondary coating. Also, the time over which the stress is exerted has an influence because relaxation can reduce stresses. The latter is shown e.g. by Reddy et al., in the 1993 Proc. of the 42 nd WCS p. 386-392. A higher modulus and higher Tg secondary coating will cause greater stress on the primary. Hence, it is preferred that the cavitation strength of the primary coating at which the tenth cavitation ⁇ 10 cav appears is about 1.1 MPa or more, and most preferred about 1.2 MPa or more.
  • the present invention further relates to a coated optical fiber comprising a glass optical fiber, a primary coating applied thereon, a secondary coating and optionally an ink composition subsequently applied thereon, wherein the primary coating is as defined above.
  • a coating should preferably have a strain hardening behavior, and the coating preferably should have a certain strain energy release rate (Go).
  • Strain hardening can be defined by the behavior of a coating in a tensile test resulting in a stress-strain curve that deviates from an "ideal rubber"-profile.
  • Strain hardening can be measured by a stress-strain curve, and is preferably defined by a curve in a relative Mooney plot (see Figure 5), as described below.
  • a relative Mooney plot can be obtained as follows:
  • the primary measurement is the force-displacement curve, measured according to ISO 37 with a speed of 5mm/min, preferably 50 mm/min, and more preferred 500 mm/min. At higher speed, it is more certain that the effect of the material can be measured, in particular, when the strain hardening behaviour sets in only at higher strain.
  • a Mooney plot can now be constructed by plotting ⁇ M versus 1/ ⁇ .
  • a strain hardening material shows an increase in the relatively Mooney stress at lower values of 1/ ⁇ .
  • the relative Mooney plot can now be constructed by plotting ⁇ rM versus 1/ ⁇ .
  • L ( x ) coth( x ) - 1 x
  • the constants a and b are respectively 0.94 and 11.20.
  • the primary coatings showing strain hardening according to the present invention show a curve in the relative Mooney plot which increases on lowering 1/ ⁇ and of which at least one point has a value higher than the value calculated by using the function f( ⁇ ) for 1/ ⁇ of about 0.60 or less.
  • f( ⁇ ) preferably applies for 1/ ⁇ of about 0.55 or less, more preferably, for 1/ ⁇ of about 0.50 or less.
  • the strain hardening behavior of a primary coating is more effective in preventing cavities if the strain hardening occurs at lower elongation (or higher 1/ ⁇ ).
  • the present inventors have used an uniaxial stretching test wherein the coating test specimen is pulled in uniaxial direction according to ISO 37 under the conditions as described in the experimental section.
  • the strain energy release rate or tear strength (Go) is the energy required per 1m 2 of crack surface in a test specimen of a cured primary coating initially containing a small crack equal to the slit length b as defined in ISO 816.
  • the strain energy release rate Go depends on the strain rate in a similar manner as the cavitation strength.
  • the strain energy release rate is preferably at least about 20 J/m 2 , as measured at a rate of about 1.10 -5 s -1 or less.
  • a higher tear strength aids in precluding the occurring of cavities, in particular if the coating already shows some strain hardening behavior.
  • a tear strength Go of over about 150 J/m 2 generally does not further increase the cavitation strength of a coating.
  • the tear strength preferably is about 30 J/m 2 or more, more preferably about 35 J/m 2 or more, particularly preferred about 40 J/m 2 or more, and most preferred about 45 J/m 2 or more.
  • the primary coating has an equilibrium modulus of about 1.0 MPa or less, more preferably about 0.9 MPa or less, and most preferred about 0.8 MPa or less.
  • this invention allows for the design of coating systems in which the secondary coating has a high Tg and/or high dynamic modulus at 23°C and the primary has a (very) low equilibrium modulus (preferably, about 1.0 MPa or less, more preferably about 0.9 MPa or less, even more preferred about 0.8 MPa or less).
  • the Tg of primary coatings generally is less than about 0°C, preferably, less than about -5°C, more preferred, less than about -10°C, and most preferred, less than about -20°C (as measured by the first peak tan- ⁇ at 1 Hz in a DMA curve when starting from the high temperature side).
  • the Tg of primary coatings is at least about -80°C, preferably at least about -60°C.
  • the Tg of the secondary (as measured by the peak tan- ⁇ in DMTA) is about 40°C or higher.
  • the Tg is about 50°C or higher, and more preferable about 60°C or higher.
  • the Tg will be about 100°C or lower.
  • the storage modulus E' at 23°C preferably is about 200 MPa or higher, more preferably between 400-3000 MPa.
  • the primary coating generally will be a radiation curable coating based on (meth)acrylate functional oligomers and radiation-curable monomers with photoinitiator(s) and additives.
  • additives include a stabiliser and a silane coupling agent.
  • the adhesion to the glass as measured according to adhesion test described in WO 99/15473, which is incorporated herein by reference, generally is at least about 5 g in force at 50% RH and 95% RH (Relative Humidity).
  • the adhesion is at least about 10 g in force, both at 50 RH and 95% RH.
  • the adhesion may be as high as 150 g in force.
  • the radiation curable coatings of the present invention generally comprise
  • the oligomer (A) is a urethane (meth)acrylate oligomer, comprising a (meth)acrylate group, urethane groups and a backbone.
  • (Meth)acrylate includes acrylate as well as methacrylate functionality.
  • the backbone is derived from a polyol which has been reacted with a diisocyanate and hydroxy alkyl acrylate.
  • urethane-free ethylenically unsaturated oligomers may also be used.
  • suitable polyols are polyether polyols, polyester polyols, polycarbonate polyols, polycaprolactone polyols, acrylic polyols, and the like. These polyols may be used either individually or in combinations of two or more. There are no specific limitations to the manner of polymerization of the structural units in these polyols. Any of random polymerization, block polymerization, or graft polymerization is acceptable. Examples of suitable polyols, polyisocyanates and hydroxylgroup-containing (meth)acrylates are disclosed in WO 00/18696, which is incorporated herein by reference.
  • the reduced number average molecular weight derived from the hydroxyl number of these polyols is usually from about 50 to about 25,000, preferably from about 500 to about 15,000, and more preferably from about 1,000 to about 8,000.
  • the ratio of polyol, di- or polyisocyanate (as disclosed in WO 00/18696), and hydroxyl group-containing (meth)acrylate used for preparing the urethane (meth)acrylate is determined so that about 1.1 to about 3 equivalents of an isocyanate group included in the polyisocyanate and about 0.1 to about 1.5 equivalents of a hydroxyl group included in the hydroxyl group-containing (meth)acrylate are used for one equivalent of the hydroxyl group included in the polyol.
  • an urethanization catalyst such as copper naphthenate, cobalt naphthenate, zinc naphthenate, di-n-butyl tin dilaurate, triethylamine, and triethylenediamine, 2-methyltriethyleneamine, is usually used in an amount from about 0.01 to about 1 wt% of the total amount of the reactant.
  • the reaction is carried out at a temperature from about 10 to about 90°C, and preferably from about 30 to about 80°C.
  • the number average molecular weight of the urethane (meth)acrylate used in the composition of the present invention is preferably in the range from about 1,200 to about 20,000, and more preferably from about 2,200 to about 10,000. If the number average molecular weight of the urethane (meth)acrylate is less than about 100, the resin composition tends to vitrify at room temperature; on the other hand, if the number average molecular weight is larger than about 20,000, the viscosity of the composition becomes high, making handling of the composition difficult.
  • the urethane (meth)acrylate is preferably present in an amount from about 20 to about 80 wt%, of the total amount of the resin composition.
  • the range from about 20 to about 80 wt% is particularly preferable to ensure excellent coatability, as well as superior flexibility and long-term reliability of the cured coating.
  • Preferred oligomers are polyether based acrylate oligomers, polycarbonate acrylate oligomers, polyester acrylate oligomers, alkyd acrylate oligomers and acrylated acrylic oligomers. More preferred are the urethane-containing oligomers thereof. Even more preferred are polyether urethane acrylate oligomers and urethane acrylate oligomers using blends of the above polyols, and particularly preferred are aliphatic polyether urethane acrylate oligomers.
  • the term "aliphatic" refers to a wholly aliphatic polyisocyanate used.
  • urethane-free acrylate oligomers such as urethane-free acrylated acrylic oligomers, urethane-free polyester acrylate oligomers and urethane-free alkyd acrylate oligomers are preferred.
  • Suitable reactive diluents (B) are polymerizable monofunctional vinyl monomers and polymerizable polyfunctional vinyl monomers.
  • These polymerizable vinyl monomers are preferably used in an amount from about 10 to about 70 wt%, and more preferred from about 15 to about 60 wt%, of the total amount of the resin composition.
  • Preferred reactive diluents are alkoxylated alkyl substituted phenol acrylate, such as ethoxylated nonyl phenol acrylate, vinyl monomers such as vinyl caprolactam, isodecyl acrylate, and alkoxylated bisphenol A diacrylate such as ethoxylated bisphenol A diacrylate.
  • the photoinitiators (C) are free radical photoinitiators.
  • Free-radical photoinitiators are generally divided into two classes according to the process by which the initiating radicals are formed. Compounds that undergo unimolecular bond cleavage upon irradiation are termed Type I or homolytic photoinitiators.
  • Type II photoinitiator If the excited state photoinitiator interacts with a second molecule (a coinitiator) to generate radicals in a bimolecular reaction, the initiating system is termed a Type II photoinitiator.
  • the two main reaction pathways for Type II photoinitiators are hydrogen abstraction by the excited initiator or photoinduced electron transfer, followed by fragmentation.
  • the total amount of photoinitiators present is between about 0.10 wt.% and about 20.0 wt.% relative to the total amount of the coating composition. More preferably, the total amount is at least about 0.5 wt.%, particularly preferred, at least about 1.0 wt.%, and most preferred, at least about 2.0 wt.%. Moreover, the total amount is preferably less than about 15.0 wt.%, more preferably, less than about 10.0 wt.%, and particularly preferred, less than about 6.0 wt.%
  • At least one of the photoinitiators contains a phosphorous, sulfur or nitrogen atom. It is even more preferred that the photoinitiator package comprises at least a combination of a photoinitiator containing a phosphorous atom and a photoinitiator containing a sulfur atom.
  • At least one of the compounds (C) is an oligomeric or polymeric photoinitiator.
  • an amine compound can be added to the liquid curable resin composition of the present invention to prevent generation of hydrogen gas, which causes transmission loss in the optical fibers.
  • the amine which can be used here, diallylamine, diisopropylamine, diethylamine, diethylhexylamine, and the like can be given.
  • additives such as antioxidants, UV absorbers, light stabilizers, silane coupling agents, coating surface improvers, heat polymerization inhibitors, leveling agents, surfactants, colorants, preservatives, plasticizers, lubricants, solvents, fillers, aging preventives, and wettability improvers can be used in the liquid curable resin composition of the present invention, as required.
  • the description can also apply to colored primary coating compositions.
  • the colorant can be a pigment or dye, preferably, a dye.
  • Radiation curable primary coating compositions are described in for example: EP-A-0565798, EP-A2-0566801, EP-A-0895606, EP-A-0835606 and EP-A-0894277.
  • the zero shear viscosity at 23°C of the liquid curable resin composition of the present invention is usually in the range from about 0.2 to about 200 Pa.s, and preferably from about 2 to about 15 Pa.s.
  • the elongation-at-break of the primary coatings of the present invention is typically greater than about 50%, preferably greater than about 60%, more preferably the elongation-at-break is at least about 100%, more preferably at least about 150% but typically not higher than about 400%.
  • This elongation-at-break can be measured at a speed of 5 mm/min, 50 mm/min or 500 mm/min respectively, preferably at 50 mm/min.
  • the elongation-at-break of the primary coatings should preferably be at least about 100%.
  • one way of improving the cavitation strength is by introducing bimodal multifunctionality of the cross-linking components, in other words, by a primary coating composition comprising at least one cross-linking component introducing bimodal multifunctionality into the system.
  • This can be achieved (a.o.) by using at least two oligomers with a different average molecular weight, preferably the average molecular weight of the one oligomer being on average 2 times higher than the molecular weight of the other oligomer, more preferably being on average at least 5 times higher, most preferred, at least 10 times higher; or -which is preferred- by using a multifunctional (for example difunctional or multifunctional) reactive diluent in an amount sufficient to achieve the desired cavitation strength characteristics.
  • EP-A-0311186 and EP-A-0167199 describe the use of 6% or 9.5% of a difunctional acrylate in a low modulus primary. However, these coatings show a decrease in equilibrium modulus after aging at 95°C for 30 days of more than 60%. Moreover, these coatings show strong yellowing upon aging under fluorescent light for 30 days. None of the references suggest anything on resistance to cavitation.
  • the primary coatings of the present invention show a decrease in equilibrium modulus after aging for 30 days at 95°C of less than 50%, preferably, less than 45%, more preferably, less than 40%.
  • their E' 1000 decreases by less than about 10°C under the above aging conditions, more preferably, less than about 7°C;
  • their E' 100 decreases by less than about 20°C under the above aging conditions, more preferably, less than about 15°C.
  • the primary coatings of the present invention show, upon aging for 30 days in fluorescent light (4 mW/cm 2 ), a non-yellowing value ⁇ E of about 20 or less, more preferably, about 15 or less.
  • the 30 days aging test was performed using a daylight L 35W/11 Lumilux lamp available from Osram, at such a distance that the energy at the surface of the coating is 4 mW/cm 2 as measured using a ML 1400 radiometer available from Miltec comprising an IL 1740B Photoresist.
  • the color change delta E value of the cured films is measured by conventional methods as disclosed in the publication entitled "A Measurement of the Contribution of UV Cured Coatings and Ink Binders Towards Color Change of UV Cured Inks" by D.M. Szum in Radtech Europe '93 Conference Proceedings (papers presented at the Radtech Europe Conference held May 2-6, 1993), the complete disclosure of which is hereby incorporated by reference.
  • This publication discloses measurements which were performed on three layer samples, whereas the samples of the present invention were single layers. The measurement involves a mathematical manipulation, FMC-2.
  • the primary coatings (75 ⁇ m films cured in nitrogen at 1 J/cm 2 using one D lamp; UV-dose determined with a "Light Bug” manufactured by International Light, Inc.; wavelengths measured 257-390 nm) show a hydrogen generation (24 hours at 80°C in argon) of about 0.3 ⁇ l/g or less, more preferred, about 0.25 ⁇ l/g or less.
  • Another preferred way of increasing the resistance against cavitation is to lower the amounts of monofunctional (low Mw) acrylates.
  • this measure is carried out in addition to introducing bimodality and thus, a certain amount of strain hardening into the coating system.
  • Both strain hardening and tear strength are increased by introducing a bimodal coating composition. It is preferred to use a sufficient amount of a difunctional component with a molecular weight of about 1000 or less to obtain the required strain hardening or tear strength.
  • the amount of low molecular weight multifunctional diluent preferably difunctional diluent, trifunctional diluent, long chain trifunctional diluent or a combination thereof] preferably is about 1.6 wt% or higher, more preferably about 1.8 wt% or higher, most preferred about 2.5 wt% or higher. Generally, the amount will be less than about 15 wt%, preferably less than about 9 wt% if the molecular weight of the difunctional diluent is less than about 500. Alkoxylated diol diacrylates are preferred in the coatings of the present invention.
  • Suitable examples of dioldiacrylates include hexanediol diacrylate, ethoxylated bisphenol-A diacrylate, tripropylene glycoldiacrylate and the like.
  • the at least one oligomer preferably has a molecular weight of about 4000 or more, more in particular of about 5000 or more. Generally, in view of viscosity requirements, the molecular weight is about 20,000 or less, preferably about 15,000 or less, more preferably about 10,000 or less. Any oligomer can be used, but wholly aliphatic polyether urethane oligomers are preferred. Also, polyether/polyester and polyether/polycarbonate combined urethane acrylate oligomers are preferred.
  • the resistance to cavitation can also be improved by a two step curing process, in which the coating is partly cured with a very low first dose (5-50 mJ/cm 2 ), and thereafter cured with a dose of at least about 50 mJ/cm 2 .
  • the time period between the first and second dose preferably is 2-120 sec.
  • the time period between the first and subsequent doses preferably is much shorter, preferably between 1.10 -3 and 5 sec. Therefore, the time period between the first and subsequent doses preferably is between about 1.10 -3 and about 120 sec. It is preferred to pre-cure the coating with one or more short flashes of a UV-source resulting in a total in dose of about 0.01 J/cm 2 or less (see Figure 4).
  • the following UV-source is generally used for applying the dose of more than 50 mJ/cm 2 : a Fusion F600W system having as lamps 1600M radiator (600 W/inch which equals 240 W/cm, and thus, in total 6000 W) fitted with R500 reflector one, with a H bulb and one with a D bulb. For the purposes of our invention, only the D-lamp is used to cure the samples.
  • a laboratory Macam lamp that is a 400W metal halide lamp (Macam, Flexicure system) is used to pre-cure the film with short preflashes.
  • UV light is fed into the cell by a liquid filled light guide, resulting in a cut-off of the wavelengths below 260 nm (having a wavelength shorter than 260 nm).
  • the precure is performed with a first lamp having a different spectrum than the second lamp.
  • this first lamp can be the lamp or lamps that cure the primary coating before applying the secondary coating.
  • the present invention relates to a method for curing a primary coating composition
  • a method for curing a primary coating composition comprising the steps of preparing a primary coating composition, which when cured without preflash is having an equilibrium modulus of about 1.5 MPa or less and a cavitation strength at which a tenth cavitation appears ( ⁇ 10 cav ) of at least about 0.9 MPa (preferably at least about 1.0 MPa) as measured at a deformation rate of 0.20% min -1 , said cavitation strength being about 1.0 times or less (preferably, at least 1.1.
  • said first dose comprises at least one flash of UV-light having a cut-off of the wavelengths below 260 nm, preferably below 250 nm.
  • the second UV-dose preferably does not contain a cut-off of the lower wavelengths, and thus, also contains wavelengths extending below 260 nm, more preferred below 250 nm, most preferred below 240 nm.
  • Another aspect of the present invention relates to a method for decreasing the volumetric thermal expansion coefficient of the low modulus primary coatings of the present invention, to a method for tuning the volumetric thermal expansion coefficients of both the primary and secondary coatings that are used together as a system, and to such improved primary coatings as such.
  • the volumetric thermal expansion coefficient ⁇ glass of the secondary coating can be defined as the expansion coefficient of the secondary coating in the plateau region of the volumetric expansion coefficient as a function of temperature below it's Tg, preferably below about -60°C.
  • the Young's modulus and thermal expansion coefficient are not interrelated for the primary and secondary coatings of the present invention.
  • Their Young's modulus is related to the network topology of the system, or alternatively the network density of the system.
  • the thermal expansion coefficient for these systems is related to the cohesive energy density, defined as the total amount of noncovalent interactions in the system, such as hydrogen bonding or dipolar interactions.
  • the volumetric expansion coefficient is related to the polarity of the system and not to the properties of the network.
  • the expansion coefficient ⁇ equilibrium of the system can be decreased without having to increase the modulus of the primary coating system, preferably by increasing the cohesive energy density (CED) or the polarity of the system.
  • CED cohesive energy density
  • the combined primary/secondary coating system comprises a primary coating having a sufficiently low expansion coefficient ⁇ equilibrium and a secondary coating system having a sufficiently high ⁇ glass so that the stress level in the primary coating is reduced to a level below the level of the cavitation strength of the primary coating.
  • the stress level is below 0.8 MPa or below 1.2 times it's dynamic modulus at 23°C (E'23), more preferably below 0.5 MPa or below 0.9 times it's E'23, and most preferred, the combination of primary and secondary coating is chosen such that the stress level in the primary coating is approximately zero.
  • the primary coatings having an equilibrium modulus E of about 1.5 MPa or less should have a volumetric expansion coefficient ⁇ equilibrium of about 6.85 x 10 -4 K -1 or less, preferably about 6.70 x 10 -4 K -1 or less, more preferred about 6.60 x 10 -4 K -1 or less, even more preferred about 6.50 x 10 -4 K -1 or less, and most preferred about 6.30 x 10 -4 K -1 or less.
  • the volumetric expansion coefficient of the secondary coating ⁇ glass of the present invention used in combination with the primary coating of the present invention should be at least about 2.20 x 10 -4 K -1 , preferably, at least about 2.40 x 10 -4 K -1 , more preferably at least about 2.60 x 10 -4 K -1 , even more preferred about 2.80 x 10 -4 K -1 , and most preferred at least about 2.90 x 10 -4 K -1 .
  • Theoretical calculations can be performed to estimate the thermal expansion coefficient for several coatings by using a commercial software package: the module Synthia of MSI (Molecular Simulations Inc, San Diego, CA). With this package one is able to predict thermal expansion coefficients for linear polymer materials. Our coatings may be treated as linear polymers because the thermal expansion coefficient depends on polarity and not on network characteristics for the coatings of the present invention. The polarity of a network system or the linear chemical analogue is identical.
  • the MSI Synthia software has been used to calculate ⁇ equilibrium of the primary coatings A and B, results are given in Table 1.
  • the heating rate was 2.5°C, and measurements were performed from - 60°C to + 80°C. From the ⁇ L/L the volumetric expansion coefficient ⁇ equilibrium was calculated.
  • the linear thermal expansion coefficient relates to the volumetric expansion coefficient as follows: ⁇ volumetric ⁇ 3 x ⁇ linear The measurement was corrected for quartz expansion by substracting blanco curves.
  • the data for primary coatings B and C show that even upon decrease of the modulus of the primary coating system, the ⁇ equilibrium can be remained substantially unchanged, and hence, that while having a low modulus, the ⁇ equilibrium can remain low to reduce the stress on the primary coating.
  • optical fibers are coated first with a primary coating and subsequently with a secondary coating.
  • the coatings can be applied as a wet-on-wet system (without first curing of the primary) or as a wet-on-dry system.
  • the primary coating can be colored with a die, or secondary coatings can be colored with pigments or dies, or a clear secondary can be further coated with an ink.
  • the primary and secondary coatings generally have a thickness of about 30 ⁇ m each.
  • An ink coating generally has a thickness of about 5 ⁇ m (3-10 ⁇ m).
  • the coated and preferably colored optical fibers can be used in a ribbon comprising a plurality of said optical fibers, generally in a parallel arrangement.
  • the plurality of optical fibers is further coated with one or more matrix materials in order to obtain a ribbon.
  • the present invention therefore further relates to a ribbon comprising a plurality of coated and preferably colored optical fibers, generally in a parallel arrangement, said coated optical fiber comprising at least a primary coating according to the present invention and preferably a secondary coating according to the present invention.
  • the measurement set up consists of a digital tensile testing machine ZWICK 1484 with digital control and with a video camera fitted on the top (moving) plate of the machine (see Photograph 1).
  • the sample is held in place by a fixture connected to the load cell, The growth of the cavitations can then be followed in real time.
  • the parallellity of the set up is very important to allow a correct translation between the force at which cavitation starts and the actual stress level in the cured coating.
  • the stress distribution over the film will be nearly flat, the coating layer is then (approximately) subjected to a homogeneous triaxial stress level ⁇ , equal to the ratio (force/sample area).
  • the sample may experience a torque resulting in an inhomogeneous tearing of the polymer film.
  • the inhomogeneous stress distribution makes it difficult to translate the registered force signal into the actual stress in the film.
  • the parallelity can be finely adjusted using three micrometer screws on the moving plate of the tensile testing machine (Photograph 2). Circular glass plates (40 mm in diameter) were used ( Figure 2) and by using three hardened steel balls fitted to the adjustable plate one can - within the accuracy of the micrometer screws, about 1 ⁇ m - adjust the parallelity of the sample in the measurement set up.
  • the compliance of the measurement set up should be as low as possible to avoid any storage of elastic energy in the measurement set up.
  • the adjustable plate was therefore made of 15 mm thick steel resulting in a compliance of approximately 0,2 ⁇ m/N for the total set up.
  • the compliance is measured by using a welded steel sample having the same geometry as in Figure 2 and is determined from the measured force and displacement.
  • a 95% ethanol - 5% water solution was adjusted to pH 4.5 - 5.5 with acetic acid, and a silane (Methacryloxypropyltrimethoxysilane, A174 from Witco) was added to yield a 5% silane solution (ca. 74.39%wt ethanol / 3.84%wt water / 16.44%wt acetic acid / 5.32%wt silane).
  • the silane solution was left for five minutes at room temperature to allow hydrolysis and silanol formation.
  • the fresh silane solution was applied to the glass or quartz surfaces by using pipette.
  • the silane layer was cured by placing the treated glass or quartz plates in an oven at 90°C for five to ten minutes. The treated glass or quartz plates were rinsed free of excess materials by gently dipping in ethanol.
  • the example was assembled as follows: A quartz cup was attached to the top plate of the two-plate micrometer using a vacuum system (vacuum pump) (Photograph 4).
  • the micrometer was zeroed using both the quartz billet and the glass plate. A droplet of resin was gently placed in the middle of the glass plate.
  • the glass plate was placed on the lower plate of the two-plate micrometer and the film thickness was adjusted by slowly pushing the quartz billet onto the resin droplet. Subsequently, the sample was cured with a 1 J/cm 2 UV-dose of Fusion F600W UV-lamp system having as lamps 1600M radiator (600 W/inch which equals 240 W/cm, and thus, in total 6000 W) fitted with R500 reflector, one with a H bulb and one with a D bulb UV lamp, of which the D-bulb was used to cure the samples.
  • Fusion F600W UV-lamp system having as lamps 1600M radiator (600 W/inch which equals 240 W/cm, and thus, in total 6000 W) fitted with R500 reflector, one with a H bulb and one with a D bulb UV lamp, of which the D-bulb was used to cure the samples.
  • the samples were stored in a dark place, so that no post-cure by UV-light can take place.
  • the sample was placed in the tensile testing apparatus from ZWICK type 1484.
  • the samples were cured with a 1 J/cm 2 UV-dose of a Fusion F600W UV-lamp system (measured with AN international Light 390-bug) as described under paragraph A above using a D bulb at a belt speed of 20.1 m/min.
  • the equilibrium modulus of the primary coatings of the present invention is measured by DMTA in tension according to the standard Norm ASTM D5026-95a "Standard Test Method for Measuring the Dynamic Mechanical Properties of Plastics in Tension" under the following conditions which are adapted for the coatings of the present invention.
  • each sample is submitted to a strain sweep to determine the ideal strain range to be applied. Then, a temperature sweep measurement is carried out under the following conditions:
  • the lowest value of the dynamic modulus E' in the DMTA curve in the temperature range between 10 and 100 °C measured at a frequency of 1 Hz under the conditions as described in detail above is taken as the equilibrium modulus of the coating.
  • the modulus E' at 23°C in the DMTA curve is taken as E'23.
  • a relative Mooney plot can be obtained as follows:
  • the primary measurement is the force-displacement curve, measured according to International Standard ISO 37 (third edition 1994-05-15) "Rubber, vulcanised or thermoplastic - Determination of tensile stress-strain properties" which is an uniaxial tensile test.
  • ISO 37 third edition 1994-05-15
  • thermoplastic - Determination of tensile stress-strain properties which is an uniaxial tensile test.
  • the above force-displacement curve is measured using a clamp displacement speed of 5mm/min, 50mm/min or 500mm/min.
  • a clamp displacement speed of 5mm/min, 50mm/min or 500mm/min.
  • the effect of the material can be visualized better, in particular in case of materials for which the strain hardening sets in only at higher strain.
  • the engineering stress is calculated according to formulas (1)-(6) as given in the description.
  • the strain energy release rate Go is measured according to the International Standard norm ISO 816 (second edition 1983-12-01) "Rubber, vulcanized - Determination of tear strength of small test pieces (Delft test pieces)" under the following specific conditions:
  • the adhesion of cured samples on a glass plate at 50% relative humidity and 95% relative humidity were tested using a universal testing instrument, INSTRON Model TTD.
  • the load cell had a ten pound (3732gram) capacity.
  • Glass plates, polished, 20 X 20 cm, (Alletch Associates catalog number 26080) were used.
  • the test material was applied to the glass plates and cured at 1 J/ cm 2 with a Fusion D Lamp under Nitrogen atmosphere. The thickness of the cured film was about 75 microns.
  • the cured films were held at 50% relative humidity, at about 23°C, for seven days prior to testing.
  • Test specimens approximately 25.4 mm in width and 127 mm long, were cut parallel to the direction in which the drawdown of the cured film was prepared. A thin layer of talc was applied to the first and third strips on each drawdown to reduce blocking during the adhesion test.
  • the instrument was calibrated prior to testing.
  • the crosshead speed was set to 254 mm/min.
  • the force required to remove four test specimens from the glass plate was measured and recorded on a strip chart recorder. The value reported is the average of the four measured values.
  • the test specimens remaining on the glass plate were then held at 95% relative humidity, at about 23°C, in an environmental chamber for 1 more day. Prior to removing the plates from the environmental chamber, a layer of slurry (fine powdered polyethylene and water) was applied to the surface of the drawdown to retain the moisture. For each material, the force to remove four test specimens from the glass plate was measured as above.
  • a coating was prepared using 50 wt% of a polyether urethane acrylate (theoretical molecular weight ⁇ 9000), about 20 wt% of 8 times ethoxylated nonylphenol acrylate, 20 wt% laurylacrylate, 6 wt% by wt of N-vinylcaprolactam, 1.5 wt% Lucirine TPO, 0.8 wt% Irganox 1035, 0.1 wt% diethanolamine and 0.3 % Seesorb 102.
  • a polyether urethane acrylate theoretical molecular weight ⁇ 9000
  • about 20 wt% of 8 times ethoxylated nonylphenol acrylate 20 wt% laurylacrylate
  • 6 wt% by wt of N-vinylcaprolactam 6 wt% by wt of N-vinylcaprolactam
  • 1.5 wt% Lucirine TPO 0.8 wt% Irganox
  • a commercial coating with an equilibrium modulus of 1.0 MPa was used.
  • the sample was cured using a dose of 1 J/cm 2 .
  • the cavitation strength measured at the occurrence of the cavitation was 1.21 MPa.
  • the dynamic modulus E' at 23°C of the coating E'23 is 0.97 MPa.
  • Example 1 the sample was first cured with three short flashes of UV-light (in total about 1 cJ/cm 2 or less), whereafter the sample was cured at 1 J/cm 2 (as described in the Description of Test Methods above).
  • a laboratory Macam lamp which is a 400W metal halide lamp (Macam, Flexicure system) is used to pre-cure the sample (the three short flashes of 1cJ/cm 2 or less in total): UV-light is fed into the cell by a liquid filled light guide, resulting in a cut-off of the wavelengths below 260 nm.
  • the cavitation strength of the coating of Example 1 measured at the tenth cavity ⁇ 10 was 1.47 MPa and E'23 was 0.97 MPa (see Figure 3), hence, the ⁇ 10 /E' 23 was 1.52.
  • Figure 3 shows the number of cavitations observed at increasing stresses on the primary coating sample without (Comp. Experiment B) and with (Ex. 1) precure.
  • a coating was formulated using 69.7 wt% of a polyether urethane acrylate oligomer having a polyether backbone comprising on average two blocks polypropylene glycol having an average Mw of about 4000 and being end-capped with ethoxy groups (the oligomer is the reaction product of a polyether polyol, toluene diisocyanate and 2-hydroxyethyl acrylate), 20.4 wt% 2-phenoxyethyl acrylate, 6.4 wt% tripropyleneglycoldiacrylate, 0.3 wt% DC190, 0.2 wt% DC57 and 1 wt% mercapto silane.
  • the equilibrium modulus was 0.6 MPa.
  • the modulus E' at 23°C was 0.7 MPa.
  • the relative Mooney plot is given in Fig. 4.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Paints Or Removers (AREA)
  • Surface Treatment Of Glass Fibres Or Filaments (AREA)
  • Investigating Strength Of Materials By Application Of Mechanical Stress (AREA)
EP00204144A 2000-11-22 2000-11-22 Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren Withdrawn EP1209132A1 (de)

Priority Applications (24)

Application Number Priority Date Filing Date Title
EP00204144A EP1209132A1 (de) 2000-11-22 2000-11-22 Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren
CNB2006100726945A CN100545685C (zh) 2000-11-22 2001-11-21 涂覆的光导纤维
EP01997528A EP1341857B1 (de) 2000-11-22 2001-11-21 Strahlungsvernetzbare zusammensetzung
US09/989,703 US7067564B2 (en) 2000-11-22 2001-11-21 Coated optical fibers
AT01997528T ATE302823T1 (de) 2000-11-22 2001-11-21 Strahlungsvernetzbare zusammensetzung
BR0115549-0A BR0115549A (pt) 2000-11-22 2001-11-21 Composições curáveis por radiação
DE60112965T DE60112965D1 (de) 2000-11-22 2001-11-21 Strahlungsvernetzbare zusammensetzung
US09/989,717 US6916855B2 (en) 2000-11-22 2001-11-21 Radiation curable compositions
KR10-2003-7006878A KR20030055316A (ko) 2000-11-22 2001-11-21 방사선 경화성 조성물
KR1020027009364A KR100854847B1 (ko) 2000-11-22 2001-11-21 코팅된 광학섬유
AU2002222795A AU2002222795A1 (en) 2000-11-22 2001-11-21 Radiation curable compositions
CNA018221807A CN1486349A (zh) 2000-11-22 2001-11-21 辐射固化组合物
PCT/NL2001/000850 WO2002042237A2 (en) 2000-11-22 2001-11-21 Coated optical fibers
CNB018070361A CN1257003C (zh) 2000-11-22 2001-11-21 涂覆的光导纤维
JP2002545092A JP2004514759A (ja) 2000-11-22 2001-11-21 照射硬化可能な組成物
JP2002544378A JP4268406B2 (ja) 2000-11-22 2001-11-21 コーティングされた光ファイバー
EP01997468.2A EP1274662B1 (de) 2000-11-22 2001-11-21 Beschichtungzusammensetzung, Verfahren zur Härtung von Beschichtungen und beschichtete optische Fasern
PCT/NL2001/000849 WO2002042383A1 (en) 2000-11-22 2001-11-21 Radiation curable compositions
AU2002222796A AU2002222796A1 (en) 2000-11-22 2001-11-21 Coated optical fibers
US11/109,949 US20050187310A1 (en) 2000-11-22 2005-04-20 Radiation curable compositions
US11/269,765 US7706659B2 (en) 2000-11-22 2005-11-09 Coated optical fibers
JP2008139946A JP4594999B2 (ja) 2000-11-22 2008-05-28 光ファイバー用プライマリーコーティングのキャビテーション強度の測定用アセンブリ
US12/591,242 US7865055B2 (en) 2000-11-22 2009-11-13 Coated optical fibers
US12/591,241 US7886612B2 (en) 2000-11-22 2009-11-13 Coated optical fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP00204144A EP1209132A1 (de) 2000-11-22 2000-11-22 Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren

Publications (1)

Publication Number Publication Date
EP1209132A1 true EP1209132A1 (de) 2002-05-29

Family

ID=8172313

Family Applications (2)

Application Number Title Priority Date Filing Date
EP00204144A Withdrawn EP1209132A1 (de) 2000-11-22 2000-11-22 Beschichtete optische Fasern, primäre Beschichtungszusammensetzung, Härtungsverfahren, sowie ein Messungsgerät und ein Messungsverfahren
EP01997468.2A Expired - Lifetime EP1274662B1 (de) 2000-11-22 2001-11-21 Beschichtungzusammensetzung, Verfahren zur Härtung von Beschichtungen und beschichtete optische Fasern

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP01997468.2A Expired - Lifetime EP1274662B1 (de) 2000-11-22 2001-11-21 Beschichtungzusammensetzung, Verfahren zur Härtung von Beschichtungen und beschichtete optische Fasern

Country Status (6)

Country Link
EP (2) EP1209132A1 (de)
JP (2) JP4268406B2 (de)
KR (1) KR100854847B1 (de)
CN (2) CN1257003C (de)
AU (1) AU2002222796A1 (de)
WO (1) WO2002042237A2 (de)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003011938A1 (en) * 2001-07-27 2003-02-13 Corning Incorporated Low modulus, high tensile strength optical fiber coating
EP1391439A2 (de) * 2002-08-22 2004-02-25 FITEL USA CORPORATION (a Delaware Corporation) Verfahren und Vorrichtung zum Färben von optischen Fasern während des Ziehens
EP1930381A1 (de) * 2006-12-05 2008-06-11 DSMIP Assets B.V. Strahlungshärtbare Beschichtungszusammensetzung
EP2026110A1 (de) * 2006-06-02 2009-02-18 The Furukawa Electric Co., Ltd. Optischer faserkern und verfahren zu seiner bewertung
EP2051119A1 (de) * 2006-08-10 2009-04-22 The Furukawa Electric Co., Ltd. Optische faser
WO2010121659A1 (en) * 2009-04-23 2010-10-28 Prysmian S.P.A. Optical fiber with single coating
US20210103092A1 (en) * 2019-10-08 2021-04-08 Corning Incorporated Primary coating compositions with improved microbending performance

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004010179A1 (en) * 2002-07-18 2004-01-29 Dsm Ip Assets B.V. Coated photonic crystal fibers
CN103232175B (zh) * 2006-12-14 2016-05-11 帝斯曼知识产权资产管理有限公司 光纤上的d1363bt可辐射固化初级涂层
KR101018357B1 (ko) * 2008-07-16 2011-03-04 에스에스씨피 주식회사 우수한 고온 내수성을 갖는 광경화형 코팅 조성물
JP5530141B2 (ja) * 2009-09-29 2014-06-25 富士フイルム株式会社 インク組成物及びインクジェット記録方法
JP5625186B2 (ja) * 2009-10-09 2014-11-19 ディーエスエム アイピー アセッツ ビー．ブイ． Ｄ１４５２ｇｂ光ファイバ用放射線硬化性被覆材
JP5959780B2 (ja) 2014-07-29 2016-08-02 古河電気工業株式会社 光ファイバ着色心線
CN106525302B (zh) * 2016-12-16 2022-03-11 善测（天津）科技有限公司 一种基于高精度键相的旋转轴扭矩非接触动态测量系统
KR20210018337A (ko) * 2018-06-01 2021-02-17 디에스엠 아이피 어셋츠 비.브이. 광섬유 코팅용 방사선 경화성 조성물 및 이로부터 제조된 코팅
JP7099160B2 (ja) * 2018-08-10 2022-07-12 住友電気工業株式会社 光ファイバの製造方法
CN109180023B (zh) * 2018-08-31 2021-01-12 江苏亨通光纤科技有限公司 一种耐高温光纤及其制备方法
KR102021420B1 (ko) * 2019-02-27 2019-09-16 우태영 광촉매 프리코트를 이용한 유리 및 알루미늄 구조체 공기필터 및 이의 제조방법

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0167199A1 (de) 1984-06-22 1986-01-08 Koninklijke Philips Electronics N.V. Optische Glasfaser mit einer Kunststoffbedeckung und Verfahren zum Herstellen derselben
EP0311186A1 (de) 1987-10-08 1989-04-12 Koninklijke Philips Electronics N.V. Optische Faser mit einer Kunststoffbedeckung
WO1991003499A1 (en) 1989-09-06 1991-03-21 Desoto, Inc. Primary coatings for optical glass fibers including polyether acrylates
EP0565798A1 (de) 1992-04-16 1993-10-20 Borden, Inc. UV-Strahlungshärtbare Beschichtung für optische Fasern und damit beschichtete optische Fasern
EP0566801A2 (de) 1992-04-24 1993-10-27 Borden, Inc. Organische Lösungsmittel und wasserresistente, thermisch, oxidatif und hydrolytisch stabile strahlenhärtbare Beschichtungen für optische Fasern, damit beschichtete optische Fasern und Verfahren zur deren Herstellung
WO1997042130A1 (en) 1996-05-07 1997-11-13 Dsm N.V. A method of making a radiation-curable, optical glass fiber coating composition having extended shelf life and said composition
EP0835606A1 (de) 1992-11-17 1998-04-15 Novartis AG Synergistische mikrobizide Mittel
US5744514A (en) * 1996-10-31 1998-04-28 Borden Chemical, Inc. Coated optical fibers having a reduced content of extractable and volatile material
US5837750A (en) * 1995-03-13 1998-11-17 Dsm N.V. Radiation curable optical fiber coating composition
EP0894277A1 (de) 1997-01-24 1999-02-03 Borden Chemical, Inc. Beschichtete optische fasern mit abziehbaren primärbeschichtungen und herstellungsverfahren und verwendung
WO1999008975A1 (en) 1997-08-15 1999-02-25 Dsm N.V. Radiation-curable resin composition
WO1999015473A1 (en) 1997-09-22 1999-04-01 Dsm N.V. Radiation-curable compositions having fast cure speed and good adhesion to glass
WO1999052958A1 (en) * 1998-04-15 1999-10-21 Dsm N.V. Radiation curable resin composition
WO2000018696A1 (en) 1998-09-30 2000-04-06 Dsm N.V. Radiation-curable composition
US6110593A (en) * 1998-05-21 2000-08-29 Dsm N.V. Radiation-curable optical fiber primary coating system

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05249028A (ja) * 1992-03-06 1993-09-28 Kansai Paint Co Ltd 塗膜の接着力測定試験機
US6215934B1 (en) * 1998-10-01 2001-04-10 Lucent Technologies, Inc. Coated optical fiber with improved strippability
JP2000121464A (ja) * 1998-10-15 2000-04-28 Ricoh Co Ltd 樹脂成形体の密着力測定装置

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0167199A1 (de) 1984-06-22 1986-01-08 Koninklijke Philips Electronics N.V. Optische Glasfaser mit einer Kunststoffbedeckung und Verfahren zum Herstellen derselben
EP0311186A1 (de) 1987-10-08 1989-04-12 Koninklijke Philips Electronics N.V. Optische Faser mit einer Kunststoffbedeckung
WO1991003499A1 (en) 1989-09-06 1991-03-21 Desoto, Inc. Primary coatings for optical glass fibers including polyether acrylates
EP0565798A1 (de) 1992-04-16 1993-10-20 Borden, Inc. UV-Strahlungshärtbare Beschichtung für optische Fasern und damit beschichtete optische Fasern
EP0566801A2 (de) 1992-04-24 1993-10-27 Borden, Inc. Organische Lösungsmittel und wasserresistente, thermisch, oxidatif und hydrolytisch stabile strahlenhärtbare Beschichtungen für optische Fasern, damit beschichtete optische Fasern und Verfahren zur deren Herstellung
EP0835606A1 (de) 1992-11-17 1998-04-15 Novartis AG Synergistische mikrobizide Mittel
US5837750A (en) * 1995-03-13 1998-11-17 Dsm N.V. Radiation curable optical fiber coating composition
WO1997042130A1 (en) 1996-05-07 1997-11-13 Dsm N.V. A method of making a radiation-curable, optical glass fiber coating composition having extended shelf life and said composition
US5744514A (en) * 1996-10-31 1998-04-28 Borden Chemical, Inc. Coated optical fibers having a reduced content of extractable and volatile material
EP0895606A1 (de) 1996-10-31 1999-02-10 Borden Chemical, Inc. Beschichtete optische fasern mit reduzierter menge von extrahierbarem und flüchtigem material
EP0894277A1 (de) 1997-01-24 1999-02-03 Borden Chemical, Inc. Beschichtete optische fasern mit abziehbaren primärbeschichtungen und herstellungsverfahren und verwendung
WO1999008975A1 (en) 1997-08-15 1999-02-25 Dsm N.V. Radiation-curable resin composition
WO1999015473A1 (en) 1997-09-22 1999-04-01 Dsm N.V. Radiation-curable compositions having fast cure speed and good adhesion to glass
WO1999052958A1 (en) * 1998-04-15 1999-10-21 Dsm N.V. Radiation curable resin composition
US6110593A (en) * 1998-05-21 2000-08-29 Dsm N.V. Radiation-curable optical fiber primary coating system
WO2000018696A1 (en) 1998-09-30 2000-04-06 Dsm N.V. Radiation-curable composition

Non-Patent Citations (10)

* Cited by examiner, † Cited by third party
Title
"ACS SYMPOSIUM SERIES 193", 1982, AMERICAN CHEMICAL SOCIETY, WASHINGTON DC, article J.E. MARK ET AL: "Elastomers and Rubber Elasticity"
"L.R.G. TRELOAR", part 2 EDT 1967, OXFORD AT CLAREDON PRESS, article "The Physics of Rubber elasticity"
A MEASUREMENT OF THE CONTRIBUTION OF UV CURED COATINGS AND INK BINDERS TOWARDS COLOR CHANGE OFUV CURED INKS, D.M. Szum, Radtech Europe '93 Conference Proceedings
BOUTEN ET AL., JOURNAL OF LIGHTWAVE TECHNOLOGY, vol. 7, April 1989 (1989-04-01), pages 680 - 686
DE VRIES ET AL: "Polymer Symposium", JOURNAL OF POLYMER SCIENCE, vol. 58, 1977, pages 109 - 156
KING AND ALOISIO: "Thermomechnical Mechanism for Delamination of Polymer Coatings from Optical Fibers", JOURNAL ELECTRONIC PACKAGING, vol. 119, June 1997 (1997-06-01), pages 133 - 137
M.H. ALY ET AL, J. OPT. COMMUN., vol. 2, no. 82, 1998
MORI et al., RAD TECH PROCEEDINGS 1998, USA
PROC. OF THE 42ND WCS, 1993, article REDDY ET AL, pages: 386 - 392
SUHIR E., J. LIGHTWAVE TECHNOLOGY, vol. 8, no. 863, 1990

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003011938A1 (en) * 2001-07-27 2003-02-13 Corning Incorporated Low modulus, high tensile strength optical fiber coating
EP1391439A2 (de) * 2002-08-22 2004-02-25 FITEL USA CORPORATION (a Delaware Corporation) Verfahren und Vorrichtung zum Färben von optischen Fasern während des Ziehens
EP1391439A3 (de) * 2002-08-22 2004-11-17 FITEL USA CORPORATION (a Delaware Corporation) Verfahren und Vorrichtung zum Färben von optischen Fasern während des Ziehens
EP2026110A1 (de) * 2006-06-02 2009-02-18 The Furukawa Electric Co., Ltd. Optischer faserkern und verfahren zu seiner bewertung
EP2026110A4 (de) * 2006-06-02 2013-05-08 Furukawa Electric Co Ltd Optischer faserkern und verfahren zu seiner bewertung
EP2051119A4 (de) * 2006-08-10 2013-11-06 Furukawa Electric Co Ltd Optische faser
EP2051119A1 (de) * 2006-08-10 2009-04-22 The Furukawa Electric Co., Ltd. Optische faser
WO2008069656A1 (en) * 2006-12-05 2008-06-12 Dsm Ip Assets B.V. Radiation-curable coating composition
EP1930381A1 (de) * 2006-12-05 2008-06-11 DSMIP Assets B.V. Strahlungshärtbare Beschichtungszusammensetzung
WO2010121659A1 (en) * 2009-04-23 2010-10-28 Prysmian S.P.A. Optical fiber with single coating
US8792761B2 (en) 2009-04-23 2014-07-29 Prysmian S.P.A. Optical fiber with single coating
US20210103092A1 (en) * 2019-10-08 2021-04-08 Corning Incorporated Primary coating compositions with improved microbending performance
US11822117B2 (en) * 2019-10-08 2023-11-21 Corning Incorporated Primary coating compositions with improved microbending performance

Also Published As

Publication number Publication date
AU2002222796A1 (en) 2002-06-03
WO2002042237A3 (en) 2002-10-03
KR100854847B1 (ko) 2008-08-27
CN100545685C (zh) 2009-09-30
EP1274662A2 (de) 2003-01-15
CN1257003C (zh) 2006-05-24
WO2002042237A2 (en) 2002-05-30
JP2008275631A (ja) 2008-11-13
JP2004514745A (ja) 2004-05-20
JP4594999B2 (ja) 2010-12-08
KR20020087395A (ko) 2002-11-22
CN1419470A (zh) 2003-05-21
JP4268406B2 (ja) 2009-05-27
CN1841102A (zh) 2006-10-04
EP1274662B1 (de) 2015-09-02

Similar Documents

Publication Publication Date Title
US7067564B2 (en) Coated optical fibers
US7865055B2 (en) Coated optical fibers
JP4594999B2 (ja) 光ファイバー用プライマリーコーティングのキャビテーション強度の測定用アセンブリ
US7221842B2 (en) Coated optical fiber and optical fiber coating system including a fast-gelling primary coating
KR101053943B1 (ko) 코팅된 광섬유
EP1178064B1 (de) Schnell aushärtende strahlungshärtbare Zusammensetzung und damit beschichteter optischer Wellenleiter
DE69833322T2 (de) Eine ein urethan-oligomer mit einem polyestergerüst enthaltende strahlungshärtbare zusamensetzung
KR101104971B1 (ko) 광섬유용 ｄ1369 ｄ 방사선 경화성 2차 코팅
KR101334427B1 (ko) 방사선-경화성 코팅 조성물
WO2005026228A1 (en) Curable liquid resine composition
CN113711096A (zh) 包层厚度减小的多模光纤
US20070263972A1 (en) Optical Fiber with Cured Polymeric Coating
EP0863854B1 (de) Flüssige photohärtbare harzzusammensetzung
US20030215196A1 (en) Coated optical fibers
CN112437761A (zh) 用于涂覆光纤的辐射可固化组合物及由其生产的涂层
US9563013B2 (en) Primary coatings for optical fibers having short gel times
US6872760B2 (en) Radiation-curable composition for optical fiber coating materials
CN114845967A (zh) 具有低拔出力的光纤涂层

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

AKX Designation fees paid
REG Reference to a national code

Ref country code: DE

Ref legal event code: 8566

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20021130